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Study of GS-0272 in Participants With Rheumatoid Arthritis

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NCT06031415

Sponsored by Gilead Sciences (industry) · GILD — their whole pipeline →.

Phase
Phase 1
Status
Terminated
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
55actual
Sites
24
Countries
Georgia, Moldova, South Korea +2

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

Study terminated due to lack of efficacy.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-09-28actualWhen the study began enrolling
Primary completion2026-05-11actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-05-11actualThe whole study's end, after follow-up
First posted2023-09-11actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-27actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Rheumatoid Arthritis

Interventions

  • Drug: GS-0272
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Percentage of Participants Experiencing Adverse Events (AEs)
measured First dose up to Week 12 plus 70 days
Percentage of Participants Experiencing Serious Adverse Events (SAEs)
measured First dose up to Week 12 plus 70 days
Percentage of Participants With Laboratory Abnormalities
measured First dose up to Week 12 plus 70 days
Pharmacokinetics (PK) of GS-0272: AUCtau
measured Day 1 predose through Day 197
PK of GS-0272: Cmax
measured Day 1 predose through Day 197
PK of GS-0272: Tmax
measured Day 1 predose through Day 197

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